Canonical Allele Identifier: CA278243172
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs985512634
gnomAD v3: 16-11310061-G-A
gnomAD v4: 16-11310061-G-A
MyVariant Identifiers: chr16:g.11403918G>A (hg19) chr16:g.11310061G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11310061G>A , CM000678.2:g.11310061G>A GRCh38
NC_000016.9:g.11403918G>A , CM000678.1:g.11403918G>A GRCh37
NC_000016.8:g.11311419G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+60283G>A
ENST00000572173.1:c.-436-2768G>A ENSP00000461206.1:n.-436-2768G>A
ENST00000573910.1:n.161-6391G>A
XR_933070.1:n.733+60283G>A
XR_933070.3:n.876+60283G>A
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